|Número de publicación||US20060149348 A1|
|Tipo de publicación||Solicitud|
|Número de solicitud||US 11/363,426|
|Fecha de publicación||6 Jul 2006|
|Fecha de presentación||27 Feb 2006|
|Fecha de prioridad||27 Nov 2003|
|También publicado como||DE10355986A1, EP1686928A1, US8388616, WO2005051238A1|
|Número de publicación||11363426, 363426, US 2006/0149348 A1, US 2006/149348 A1, US 20060149348 A1, US 20060149348A1, US 2006149348 A1, US 2006149348A1, US-A1-20060149348, US-A1-2006149348, US2006/0149348A1, US2006/149348A1, US20060149348 A1, US20060149348A1, US2006149348 A1, US2006149348A1|
|Inventores||Bernd Vogel, Harald Fischer, Marco Klein|
|Cesionario original||Bernd Vogel, Harald Fischer, Marco Klein|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (37), Citada por (16), Clasificaciones (18), Eventos legales (3)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
This is a Continuation-In-Part Application of International Application PCT/EP2004/013303 filed Nov. 24, 2004 and claiming the priority of German application 103 55 986.8 filed Nov. 27, 2003.
The invention relates to a compression sleeve for enshrouding a blood vessel or a vein valve area.
Weak tissues in a human body, in particular blood vessel tissue, will lead with increasing age to significant vessel expansions. This effect is particularly prominent when a body's valve systems in the blood circuit are expanded to such an extent that they do not work any more properly as unidirectional valves (check valves or flow control valves) so that backflow occurs at the valves and the blood vessels are exposed to additional internal pressures loads.
Without treatment, this effect results in the formation of varicose veins. Such veins are first formed by a widening of the blood vessels particularly in weak or resilient tissue areas or vessel walls. As a result, also the vein valves in the body for example in the area of the pelvis may expand and, in time, these valves generally fail. Finally, enhanced by the gravity, blood backup occurs resulting in further pressure exposure and further expansion of the veins, particularly in the legs. The dilation of the veins results first in varicose veins and finally in open legs.
These symptoms are treated by the use of support leggings which surround and compress the leg so that a counter pressure to the blood pressure is established and the blood vessel tissue stresses are relieved. However, the functionality of the vein valves of the body is not restored thereby.
For a lasting or preventative treatment of varicose veins however, it is important that the functionality of the veins and the vein valves is maintained or re-established. To avoid a dilation of veins or vein valves, it is necessary to reinforce the dilated vein tissue.
U.S. Pat. No. 5,500,014 discloses several embodiments of a support sleeve for blood vessels which are all tubular. As a result, for the installation of the sleeve, the blood vein has to be threaded through the vein that is, it first has to be cut. Furthermore, the support sleeves disclosed in this patent are not designed for growing rapidly together with the tissue of the veins.
It is therefore the object of the present invention to provide a compression sleeve which can be implanted without the need for cutting the vein and which is basically suitable for rapid growth into the vein tissue.
In a compression sleeve for the local enclosure of a blood vessel or vein area comprising a support structure of a biocompatible material, the retaining structure is a flexible mat consisting of a mesh or net-like structure provided with a structure for holding the retaining structure in a vein enclosing position.
The mat forms a compression sleeve which may be for example of titanium or titanium nickel alloys and which is wrapped around the blood vessel particularly in the area where the tissue is weak or in the area of a vein valve.
It is important that the compression sleeve is formed from a flat mat. For the installation of the sleeve, it is therefore not necessary to first cut the vein like it is necessary for the installation of tubular sleeves but the mat is simply wrapped around the vein. For this reason, the compression sleeve also includes means which ensure that the mat remains wrapped around the vein, that is, that a mat once wrapped around a blood vein remains in place. Such means are preferably either hook structures, clamps, (separately provided or formed from the mat) or an elastic pretension of the mat or a combination of the means mentioned.
Generally, dilated blood vessels in any part of the body may lead to an aneurism that is to a locally limited blood vessel expansion which, if untreated will critically stress the tissue (pressure or stretching) so that the blood vessel may rupture and result in dangerous internal bleeding. As example, a stroke may be mentioned. Under such conditions also, the cutting of a vein for the installation of a sleeve around an endangered vein which is often in sensitive body areas (brain, heart, inner organs, arteries) is usually associated with high unpredictable risks and therefore unwarrantable. The present invention however permits the application of a sleeve around the vein by a minimally invasive procedure without the need for cutting the blood vessel even in body areas which are sensitive or difficult to access.
Another important features of the invention concerns the structure of the mat which must be so formed that it becomes ingrown into the blood vessel wall and, on the other hand, ensures deformability of the applied compression sleeve. For that reason, the mat is in the form of a mesh, a netlike structure, or an open porosity structure. With a net-like structure, the mat may consist of a metal sheet or a foil which is structured by known structuring processes such as laser cutting, etching or erosion methods.
It is also within the scope of the present invention to use a mat consisting of an electrically non-conductive material wherein the webs of the mat or of parts thereof have a metallic electrically conductive core. In this way, for example, certain electrical conductor configurations can be provided on the map.
Preferably, the mat consists of a shape memory material for example a bio-compatible shape memory alloy (preferably nickel titanium alloy such as Nitanol®). With the respective material properties, two possible application variants can be realized. Both variants are equally suitable for an advantageous minimally invasive application of the compression sleeve.
In a first application variant, the predetermined superelasticity of the shape memory alloys is utilized. A mat preset in a rolled together state is elastically bent open for the installation around a blood vessel and surrounds the blood vessel simply by its elastic relaxation.
Alternatively, in a second application variant, a thermal shape memory effect of the shape memory alloy is utilized for the application of the compression sleeve. The shape memory alloy is selected under the consideration that, at a body temperature of 30 to 45° C., it has a predetermined shape (the mat is rolled up—state A) and keeps that shape, but below a switching temperature below the body temperature (minus 1 to 30° C.), a morphological conversion of the crystal grating causes a deformation of the material (straight-line mat, state B) Such a mat can be so designed that, in the state B, that is, at a temperature below 30° C., it can be placed adjacent a blood vessel so that, upon beating, the mat assumes its rolled-up shape and surrounds the blood vessel as it assumes the shape A.
The deformation and strength of the mat forming the compression sleeve can be designed individually after the determination of the needs for the particular blood vessel and the change-over to the shape of the undamaged, that is, unexpanded blood vessel. Among others, in the area of the jointure of the vena saphena magna with the vena femoralis, (area of the cross), a compression of the vena saphena magna is necessary as soon as its diameter becomes larger than 6 mm.
In the applied state, the compression sleeve assumes the function of an external stent, that is, of a support sleeve, which prevents a dilation of the respective vessel section. If the vessel is already dilated the external stent returns the blood vessel to the original state. In this state, the operation of a natural valve disposed in the area supported by the stent is re-established.
The invention will be described on the basis of actual embodiments below with reference to the accompanying drawings.
The FIGS. 1 to 3 show each a mat of a compression sleeve comprising webs 1 and openings 2. The
The embodiments of
The embodiments as shown in
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|Clasificación de EE.UU.||623/1.1|
|Clasificación internacional||A61F2/92, A61F2/91, A61F2/915|
|Clasificación cooperativa||A61F2/91, A61F2002/91516, A61F2/915, A61F2002/91558, A61F2002/91591, A61F2002/91525, A61F2/92, A61F2/2475, A61F2230/0054, A61F2002/91541, A61F2002/91508|
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|27 Feb 2006||AS||Assignment|
Owner name: FORSCHUNGSZENTRUM KARLSRUCHE GMBH, GERMANY
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:VOGEL, BERND;FISCHER, HARALD;KLEIN, MARCO;REEL/FRAME:017629/0731
Effective date: 20060208
|11 Ene 2013||AS||Assignment|
Owner name: KARLSRUHER INSTITUT FUR TECHNOLOGIE, GERMANY
Free format text: CHANGE OF NAME;ASSIGNOR:FORSCHUNGSZENTRUM KARLSRUHE GMBH;REEL/FRAME:029820/0722
Effective date: 20100202
|21 Ene 2013||AS||Assignment|
Owner name: ENDOSMART GESELLSCHAFT FUR MEDIZINTECHNIK MBH, GE
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:FORSCHUNGSZENTRUM KARLSRUHE , NOW: KARLSRUHER INSTITUT FUR TECHNOLOGIE;REEL/FRAME:029663/0360
Effective date: 20130111